HotDog Warming Mattress + Return Electrode

FDA 510(k) K230866 · Augustine Temperature Management, LLC

Substantially Equivalent

510(k) numberK230866

Submission

Device name
HotDog Warming Mattress + Return Electrode
Applicant
Augustine Temperature Management, LLC
Minneapolis, MN, US
Received
March 29, 2023
Decision date
June 29, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DWJ – System, Thermal Regulating
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5900
Specialty
Cardiovascular

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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K260903Hot Pink Pad Warming SystemDWJ · Traditional Xodus Medical, Inc.04/16/2026SE
K252861Warming SystemDWJ · Traditional Hangzhou Tappa Medical Technology Co., Ltd.04/07/2026SE
K251974Arctic Sun Temperature Management System (Model 5000)DWJ · Traditional Medivance, Inc.10/24/2025SE
K242964Celsi WarmerDWJ · Traditional Hadleigh Health Technologies06/20/2025SE
K243942Arctic Sun Stat Temperature Management SystemDWJ · Traditional Medivance, Inc.04/30/2025SE
K232627HotDog Warming Mattress + Return ElectrodeDWJ · Special Augustine Temperature Management, LLC04/18/2024SE
K232502Cocoon Convective Warming System, Model CWS7000DWJ · Traditional Care Essentials Pty, Ltd.02/21/2024SE

More from Care Essentials Pty, Ltd.

510(k)DeviceDecision
K232627HotDog Warming Mattress + Return ElectrodeDWJ · Special 04/18/2024SE
K220941HotDog Temperature Management SystemDWJ · Traditional 09/23/2022SE
K210727HotDog Warming Mattress + Return ElectrodeGEI · Abbreviated 02/01/2022SE
K201779HotDog Temperature Management ControllerDWJ · Special 09/11/2020SE

Questions and answers

When was HotDog Warming Mattress + Return Electrode cleared by the FDA?

HotDog Warming Mattress + Return Electrode (K230866) received a 510(k) decision of Substantially Equivalent on June 29, 2023, 92 days after the submission was received.

What is the product code of K230866?

The FDA product code is DWJ – System, Thermal Regulating, a Class II (moderate risk) device regulated under 21 CFR 870.5900.